TAT Antibody (PACO05173)
- SKU:
- PACO05173
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Application:
- ELISA
- Application:
- IHC
- Antibody type:
- Polyclonal
- Conjugation:
- Unconjugated
Description
抗体名: | TAT Antibody (PACO05173) |
抗体コード: | PACO05173 |
サイズ: | 50ug |
宿主種: | Rabbit |
申し込み: | ELISA, IHC |
推奨される希釈: | ELISA:1:40000, IHC:1:100-1:300 |
反応性: | Human, Mouse, Rat |
免疫原: | Synthesized peptide derived from the Internal region of human TAT. |
憲法: | Liquid |
ストレージバッファ: | Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. |
精製方法: | The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. |
抗体のクローン性: | Polyclonal |
アイソタイプ: | IgG |
Conjugate: | Non-conjugated |
シノニム: | TAT; Tyrosine aminotransferase; TAT; L-tyrosine:2-oxoglutarate aminotransferase |
UniProt Protein Function: | TAT: Transaminase involved in tyrosine breakdown. Converts tyrosine to p-hydroxyphenylpyruvate. Can catalyze the reverse reaction, using glutamic acid, with 2-oxoglutarate as cosubstrate (in vitro). Has much lower affinity and transaminase activity towards phenylalanine. Defects in TAT are the cause of tyrosinemia type 2 (TYRO2); also known as Richner-Hanhart syndrome. TYRO2 is an inborn error of metabolism characterized by elevations of tyrosine in the blood and urine, and oculocutaneous manifestations. Typical features include palmoplantar keratosis, painful corneal ulcers, and mental retardation. Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family. |
UniProt Protein Details: | Protein type:Cofactor and Vitamin Metabolism - ubiquinone and other terpenoid-quinone biosynthesis; Mitochondrial; Amino Acid Metabolism - tyrosine; Amino Acid Metabolism - phenylalanine; EC 2.6.1.5; Amino Acid Metabolism - phenylalanine, tyrosine and tryptophan biosynthesis; Amino Acid Metabolism - cysteine and methionine; Transferase Chromosomal Location of Human Ortholog: 16q22.1 Cellular Component: mitochondrion; cytosol Molecular Function:amino acid binding; tyrosine transaminase activity; pyridoxal phosphate binding Biological Process: response to mercury ion; L-phenylalanine catabolic process; glutamate metabolic process; tyrosine catabolic process; response to glucocorticoid stimulus; biosynthetic process; response to oxidative stress; 2-oxoglutarate metabolic process Disease: Tyrosinemia, Type Ii |
NCBI Summary: | This nuclear gene encodes a mitochondrial protein tyrosine aminotransferase which is present in the liver and catalyzes the conversion of L-tyrosine into p-hydroxyphenylpyruvate. Mutations in this gene cause tyrosinemia (type II, Richner-Hanhart syndrome), a disorder accompanied by major skin and corneal lesions, with possible mental retardation. A regulator gene for tyrosine aminotransferase is X-linked. [provided by RefSeq, Jul 2008] |
UniProt Code: | P17735 |
NCBI GenInfo Identifier: | 114713 |
NCBI Gene ID: | 6898 |
NCBI Accession: | P17735.1 |
UniProt Secondary Accession: | P17735,B2R8I1, D3DWS2, |
UniProt Related Accession: | P17735 |
Molecular Weight: | 454 |
NCBI Full Name: | Tyrosine aminotransferase |
NCBI Synonym Full Names: | tyrosine aminotransferase |
NCBI Official Symbol: | TAT |
NCBI Protein Information: | tyrosine aminotransferase; tyrosine aminotransferase, cytosolic; L-tyrosine:2-oxoglutarate aminotransferase |
UniProt Protein Name: | Tyrosine aminotransferase |
UniProt Synonym Protein Names: | L-tyrosine:2-oxoglutarate aminotransferase |
Protein Family: | Tat-binding |
UniProt Gene Name: | TAT |
UniProt Entry Name: | ATTY_HUMAN |